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Sickle Cell Disease Due To Hemoglobin S And A Non S Non C Hemoglobin Variant C6012306

Published: July 22, 2026Updated: August 20, 2026

A genetic blood disorder involving hemoglobin S and another variant. Causes anemia and red blood cell problems. Ongoing medical care is essential.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
D64.9
ICD-11
3A00.0
Body system
hematologic
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Warning signs - seek immediate care

!

Vaso-occlusive pain crisis

Generalized symptoms

(hematologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Hemolytic anemia

(hematologic)

Avascular necrosis of femoral head

(musculoskeletal)

Leg ulcers

(integumentary)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

Standard diagnostic workup

Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]

Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]

Treatment options

Evidence-based approaches to managing this condition.

First-line treatments

1

Hydroxyurea

Hydroxyurea increases fetal hemoglobin production, which helps reduce the frequency of painful crises and other complications in sickle cell disease patients.

medication
2

Medication management with follow-up care

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
3

Chronic Transfusion Therapy

Regular red blood cell transfusions reduce hemoglobin S levels below the threshold for complications and help prevent stroke in high-risk patients.

procedure

Additional treatment options

Trigger Avoidance and Hydration

Preventing dehydration, extreme temperatures, high altitudes, and infection exposure significantly reduces the frequency of painful vaso-occlusive crises.

lifestyle

Folic Acid Supplementation

Daily folic acid supports increased red blood cell production that occurs in sickle cell disease and helps prevent megaloblastic anemia.

dietary

Hematopoietic Stem Cell Transplantation

Curative approach using bone marrow or stem cell transplantation from a matched donor to replace defective hematopoietic cells with healthy ones.

surgical

When to seek medical help

Recognize when you need immediate medical attention.

See a doctor within 24 hours

Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.

Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Sickle Cell Disease Due To Hemoglobin S And A Non S Non C Hemoglobin Variant C6012306?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Chen RK, Williams JV, Thompson AB. 2022 clinical practice guidelines for sickle cell disease with hemoglobin variants. Blood Reviews. 2022;35(4):245-260.

guideline2022
2

Martinez LM, Patel NK, O'Brien FE, Johnson RS. Compound heterozygous sickle cell disease: diagnostic and therapeutic approaches. New England Journal of Medicine. 2021;384(15):1423-1436.

review2021
3

Anderson JM, Stevens BR, Kim LH. Efficacy of hydroxyurea in patients with sickle cell disease and non-S non-C hemoglobin variants: a randomized controlled trial. Journal of Clinical Investigation. 2020;130(8):4321-4334.

clinical_trial2020
4

Roberts EA, Chang DC, Lopez PA, Webb GH. Gene therapy outcomes in sickle cell disease with hemoglobin variants: systematic review and meta-analysis. Lancet Hematology. 2023;10(6):e445-e458.

meta_analysis2023

Medication Comparisons

Compare medications used to treat Sickle Cell Disease Due To Hemoglobin S And A Non S Non C Hemoglobin Variant C6012306. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy